Canonical Allele Identifier: CA486093045
Gene: NPAS3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.34269565G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.33800359G>A , CM000676.2:g.33800359G>A GRCh38
NC_000014.8:g.34269565G>A , CM000676.1:g.34269565G>A GRCh37
NC_000014.7:g.33339316G>A NCBI36
NG_013036.1:g.866107G>A
NG_013036.2:g.866107G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356141.9:c.2052G>A MANE Select ENSP00000348460.4:p.Lys684=
ENST00000551634.6:c.2061G>A ENSP00000448373.2:p.Lys687=
ENST00000680362.1:c.1952G>A
ENST00000681323.1:c.793+2778G>A
ENST00000346562.6:c.1956G>A ENSP00000319610.5:p.Lys652=
ENST00000356141.8:c.2052G>A ENSP00000348460.4:p.Lys684=
ENST00000357798.9:c.2013G>A ENSP00000350446.5:p.Lys671=
ENST00000548645.5:c.1962G>A ENSP00000448916.1:p.Lys654=
ENST00000551492.5:c.2067G>A ENSP00000450392.1:p.Lys689=
ENST00000551634.5:c.1974G>A ENSP00000448373.1:p.Lys658=
NM_001164749.1:c.2052G>A NP_001158221.1:p.Lys684=
NM_001165893.1:c.1962G>A NP_001159365.1:p.Lys654=
NM_022123.2:c.1956G>A NP_071406.1:p.Lys652=
NM_173159.2:c.2013G>A NP_775182.1:p.Lys671=
XM_005267991.2:c.2073G>A XP_005268048.1:p.Lys691=
XM_005267992.2:c.2067G>A XP_005268049.1:p.Lys689=
XM_005267993.2:c.2013G>A XP_005268050.1:p.Lys671=
XM_011537067.1:c.2103G>A XP_011535369.1:p.Lys701=
XM_011537068.1:c.2094G>A XP_011535370.1:p.Lys698=
XM_011537069.1:c.2064G>A XP_011535371.1:p.Lys688=
XM_011537070.1:c.2007G>A XP_011535372.1:p.Lys669=
XM_011537071.1:c.1974G>A XP_011535373.1:p.Lys658=
XM_011537072.1:c.1953G>A XP_011535374.1:p.Lys651=
XM_011537073.1:c.1746G>A XP_011535375.1:p.Lys582=
XM_011537074.1:c.1746G>A XP_011535376.1:p.Lys582=
XM_005267991.3:c.2160G>A XP_005268048.2:p.Lys720=
XM_005267992.3:c.2154G>A XP_005268049.2:p.Lys718=
XM_011537067.2:c.2103G>A XP_011535369.1:p.Lys701=
XM_011537069.2:c.2151G>A XP_011535371.2:p.Lys717=
XM_011537070.2:c.2007G>A XP_011535372.1:p.Lys669=
XM_011537071.2:c.2061G>A XP_011535373.2:p.Lys687=
XM_011537072.2:c.1953G>A XP_011535374.1:p.Lys651=
XM_017021582.1:c.2211G>A XP_016877071.1:p.Lys737=
XM_017021583.1:c.2202G>A XP_016877072.1:p.Lys734=
XM_017021584.1:c.2121G>A XP_016877073.1:p.Lys707=
XM_017021585.1:c.2070G>A XP_016877074.1:p.Lys690=
XM_017021586.1:c.1746G>A XP_016877075.1:p.Lys582=
XM_017021587.1:c.1746G>A XP_016877076.1:p.Lys582=
XM_017021588.1:c.1746G>A XP_016877077.1:p.Lys582=
NM_001164749.2:c.2052G>A MANE Select NP_001158221.1:p.Lys684=
NM_001165893.2:c.1962G>A NP_001159365.1:p.Lys654=
NM_022123.3:c.1956G>A NP_071406.1:p.Lys652=
NM_173159.3:c.2013G>A NP_775182.1:p.Lys671=
NM_001394988.1:c.2007G>A NP_001381917.1:p.Lys669=
NM_001394989.1:c.1953G>A NP_001381918.1:p.Lys651=